Canonical Allele Identifier: PA2827954389
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1042698
ClinVar RCV Id: RCV003745316
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Gln55His
CA360612233
NM_001354897.2:c.165G>C
CA360612234
NM_001354897.2:c.165G>T